Posted today
Secret
$115,000 - $130,000
Unspecified
IT - Database
Frederick, MD (On-Site/Office)
Zachary Piper Solutions is seeking a Clinical Database Developer to support the Office of Regulated Activities (ORA) in clinical research and FDA-regulated product development. The Clinical Database Developer will support data management, database development, and technical operations across multiple clinical trials for the USAMRDC. This role is hybrid in Frederick, MD.
Responsibilities for the Clinical Database Developer include:
• Design, develop, test, validate, and maintain protocol-specific clinical data management databases using InForm GTM, Central Designer, and Oracle.
• Create and maintain mock eCRFs, Data Management Plans (DMPs), Data Validation Plans (DVPs), and essential data management documentation.
• Conduct development testing and UAT, generate validation documentation, and manage post-production database modifications.
• Provide technical support for protocol-specific databases, including logging, tracking, and resolving issues across clinical projects.
• Collaborate with regulatory, clinical, and technical teams while ensuring compliance with 21 CFR Part 11, ICH, GCP, GCDMP, and industry data standards.
Qualifications for the Clinical Database Developer include:
• Bachelor's Degree in Computer Science or related discipline (or equivalent experience)
• 5+ years of clinical database development experience
• Hands-on experience with InForm GTM, EDC systems, Central Designer, and Oracle
• Experience providing data management oversight and technical end-user support
• Experience reviewing SOPs, policies, and validation documentation
• Ability to obtain a Secret clearance
• Experience with MRDC's in-house CRDMS is a plus
• Excellent written and verbal communication skills
Compensation for the Clinical Database Developer includes:
Compensation Range: $115,000 - $130,000 depending on experience
Comprehensive Benefits: Health, Dental, Vision, 401(k), Paid Time Off
This job opens for applications on 1/22/2026. Applications for this job will be accepted for at least 30 days from the posting date.
Keywords: #LI-CR2 #LI-Hybrid Clinical Database Developer, Clinical Data Management, Data Management, InForm GTM, Oracle InForm, EDC, Electronic Data Capture, Central Designer, Oracle Clinical, CRDMS, MRDC, Clinical Research Data Management System, Clinical Trials, Clinical Study Database, Clinical Data Systems, eCRF, Electronic Case Report Forms, Data Management Plans, DMP, Data Validation Plans, DVP, UAT, User Acceptance Testing, Database Testing, Database Validation, Data Standards, CDASH, SDTM, SDTMIG, SDTMIG-MD, Controlled Terminology, MedDRA, CDISC, Clinical Data Standards, Data Integrity, Data Quality, Data Queries, Edit Checks, Query Management, Data Reconciliation, Data Review, Data Cleaning, Source Verification, Clinical Programming, SAS Datasets, Metrics Reporting, Regulatory Compliance, FDA Regulations, 21 CFR Part 11, ICH Guidelines, GCP, GCDMP, ISO 14155, IND, IDE, NDA, BLA, EUA, Product Development, Biostatistics Support, Clinical Operations Support, Clinical Systems Integration, IRT, eCOA, Central Laboratory Integration, PK Data Integration, Technical Support, Database Troubleshooting, Issue Tracking, System Validation, SOP Review, Document Control, Clinical Documentation, Medical Coding, Clinical Data Oversight, Clinical Data Lifecycle, Clinical Data Workflow, Clinical Data Architecture, Clinical Informatics, Clinical Research Technology, Clinical Systems Administrator, Clinical Database Build, Workflow Design, Form Design, Visit Design, Clinical Trial Data Capture, Clinical Trial Data Oversight, Data Governance, Clinical System Upgrades, Clinical Trial Regulations, Military Medical Research, USAMRDC, ORA, Office of Regulated Activities
Responsibilities for the Clinical Database Developer include:
• Design, develop, test, validate, and maintain protocol-specific clinical data management databases using InForm GTM, Central Designer, and Oracle.
• Create and maintain mock eCRFs, Data Management Plans (DMPs), Data Validation Plans (DVPs), and essential data management documentation.
• Conduct development testing and UAT, generate validation documentation, and manage post-production database modifications.
• Provide technical support for protocol-specific databases, including logging, tracking, and resolving issues across clinical projects.
• Collaborate with regulatory, clinical, and technical teams while ensuring compliance with 21 CFR Part 11, ICH, GCP, GCDMP, and industry data standards.
Qualifications for the Clinical Database Developer include:
• Bachelor's Degree in Computer Science or related discipline (or equivalent experience)
• 5+ years of clinical database development experience
• Hands-on experience with InForm GTM, EDC systems, Central Designer, and Oracle
• Experience providing data management oversight and technical end-user support
• Experience reviewing SOPs, policies, and validation documentation
• Ability to obtain a Secret clearance
• Experience with MRDC's in-house CRDMS is a plus
• Excellent written and verbal communication skills
Compensation for the Clinical Database Developer includes:
Compensation Range: $115,000 - $130,000 depending on experience
Comprehensive Benefits: Health, Dental, Vision, 401(k), Paid Time Off
This job opens for applications on 1/22/2026. Applications for this job will be accepted for at least 30 days from the posting date.
Keywords: #LI-CR2 #LI-Hybrid Clinical Database Developer, Clinical Data Management, Data Management, InForm GTM, Oracle InForm, EDC, Electronic Data Capture, Central Designer, Oracle Clinical, CRDMS, MRDC, Clinical Research Data Management System, Clinical Trials, Clinical Study Database, Clinical Data Systems, eCRF, Electronic Case Report Forms, Data Management Plans, DMP, Data Validation Plans, DVP, UAT, User Acceptance Testing, Database Testing, Database Validation, Data Standards, CDASH, SDTM, SDTMIG, SDTMIG-MD, Controlled Terminology, MedDRA, CDISC, Clinical Data Standards, Data Integrity, Data Quality, Data Queries, Edit Checks, Query Management, Data Reconciliation, Data Review, Data Cleaning, Source Verification, Clinical Programming, SAS Datasets, Metrics Reporting, Regulatory Compliance, FDA Regulations, 21 CFR Part 11, ICH Guidelines, GCP, GCDMP, ISO 14155, IND, IDE, NDA, BLA, EUA, Product Development, Biostatistics Support, Clinical Operations Support, Clinical Systems Integration, IRT, eCOA, Central Laboratory Integration, PK Data Integration, Technical Support, Database Troubleshooting, Issue Tracking, System Validation, SOP Review, Document Control, Clinical Documentation, Medical Coding, Clinical Data Oversight, Clinical Data Lifecycle, Clinical Data Workflow, Clinical Data Architecture, Clinical Informatics, Clinical Research Technology, Clinical Systems Administrator, Clinical Database Build, Workflow Design, Form Design, Visit Design, Clinical Trial Data Capture, Clinical Trial Data Oversight, Data Governance, Clinical System Upgrades, Clinical Trial Regulations, Military Medical Research, USAMRDC, ORA, Office of Regulated Activities
group id: 10430981
